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Displaying 12 results.
    • Journal article
    Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma.
    Jinnin, Masatoshi Medici, Damian Park, Lucy Limaye, Nisha[UCL] Liu, Yanqiu Boscolo, Elisa Bischoff, Joyce Vikkula, Miikka[UCL] Boye, Eileen Olsen, Bjorn R (2008) Nature medicine — Vol. 14, no. 11, p. 1236-46 (2008)
    • Journal article
    PTHR1 mutations associated with Ollier disease result in receptor loss of function
    Couvineau, Alain Wouters, Vinciane[UCL] Bertrand, Guylène Rouyer, Christiane Gérard, Bénédicte Boon, Laurence M.[UCL] Grandchamp, Bernard Vikkula, Miikka[UCL] Silve, Caroline (2008) Human Molecular Genetics — Vol. 17, no. 18, p. 2766-75 (2008)
    • Journal article
    Association of localized intravascular coagulopathy with venous malformations
    Dompmartin, Anne[UCL] Acher, Aurélie Thibon, Pascal Tourbach, Sébastien[UCL] Hermans, Cédric[UCL] Deneys, Véronique[UCL] Pocock, Ben[UCL] Lequerrec, Agnès Labbé, Daniel Barrellier, Marie-Thérèse Vanwijck, Romain[UCL] Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2008) Archives of Dermatology — Vol. 144, no. 7, p. 873-877 (2008)
    • Journal article
    Parkes Weber syndrome, vein of Galen aneurysmal malformation, and other fast-flow vascular anomalies are caused by RASA1 mutations
    Revencu, Nicole[UCL] Boon, Laurence M.[UCL] Mulliken, John B Enjolras, Odile Cordisco, Maria Rosa Burrows, Patricia E Clapuyt, Philippe[UCL] Hammer, Frank[UCL] Dubois, Josée Baselga, Eulalia Brancati, Francesco Carder, Robin Quintal, José Miguel Ceballos Dallapiccola, Bruno Fischer, Gayle Frieden, Ilona J Garzon, Maria Harper, John Johnson-Patel, Jennifer Labrèze, Christine Martorell, Loreto Paltiel, Harriet J Pohl, Annette Prendiville, Julie Quere, Isabelle Siegel, Dawn H Valente, Enza Maria Van Hagen, Annet Van Hest, Liselot Vaux, Keith K Vicente, Asuncion Weibel, Lisa Chitayat, David Vikkula, Miikka[UCL] (2008) Human Mutation — Vol. 29, no. 7, p. 959-965 (2008)
    • Journal article
    Alpha-cardiac actin mutations produce atrial septal defects.
    Matsson, Hans Eason, Jacqueline Bookwalter, Carol S Klar, Joakim Gustavsson, Peter Sunnegårdh, Jan Enell, Henrik Jonzon, Anders Vikkula, Miikka[UCL] Gutierrez-Roelens, Ilse[UCL] Granados-Riveron, Javier Pope, Mark Bu'Lock, Frances Cox, Jane Robinson, Thelma E Song, Feifei Brook, David J Marston, Steven Trybus, Kathleen M Dahl, Niklas (2008) Human molecular genetics — Vol. 17, no. 2, p. 256-65 (2008)
    • Journal article
    Identification of candidate regions for a novel Usher syndrome type II locus.
    Ben Rebeh, Imen Benzina, Zeineb Dhouib, Houria Hadjamor, Imen Amyere, Mustapha[UCL] Ayadi, Leila Turki, Khalil Hammami, Bouthaina Kmiha, Noureddine Kammoun, Hassen Hakim, Bochra Charfedine, Ilhem Vikkula, Miikka[UCL] Ghorbel, Abdelmonem Ayadi, Hammadi Masmoudi, Saber (2008) Molecular vision — Vol. 14, p. 1719-26 (2008)
    • Journal article
    Identification des gènes et de leurs mutations responsables des anomalies vasculaires
    Vikkula, Miikka[UCL] (2008) L'agenda cardio — Vol. 21, p. 8-12 (2008)
    • Journal article
    La génétique des anomalies vasculaires
    Aerts, Virginie[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2008) Journal du Pédiatre Belge — Vol. 10, no. 2, p. 50-55 (2008)
    • Journal article
    Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.
    Balikova, Irina Martens, Kevin Melotte, Cindy Amyere, Mustapha[UCL] Van Vooren, Steven Moreau, Yves Vetrie, David Fiegler, Heike Carter, Nigel P Liehr, Thomas Vikkula, Miikka[UCL] Matthijs, Gert Fryns, Jean-Pierre Casteels, Ingele Devriendt, Koen Vermeesch, Joris Robert (2008) American journal of human genetics — Vol. 82, no. 1, p. 181-7 (2008)
    • Journal article
    GLMN (glomulin)
    Aerts, Virginie[UCL] Brouillard, Pascal[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2008) Atlas of Genetics and Cytogenetics in Oncology and Haematology — Vol. 12, no. 1, p. 41-43 (2008)
    • Journal article
    High prevalence of SDHB mutations in head and neck paraganglioma in Belgium
    Persu, Alexandre[UCL] Hamoir, Marc[UCL] Grégoire, Vincent[UCL] Garin, Pierre[UCL] Duvivier, Etienne Reychler, Hervé[UCL] Chantrain, Gilbert[UCL] Mortier, Geert Mourad, Michel[UCL] Maiter, Dominique[UCL] Vikkula, Miikka[UCL] (2008) Journal of Hypertension — Vol. 26, no. 7, p. 1395-1401 (2008)
    • Journal article
    Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep
    Coutelier, M. Andries, Sybille[UCL] Ghariani, Sophie[UCL] Dan, B. Duyckaerts, C. Van Rijckevorsel, Kenou[UCL] Raftopoulos, Christian[UCL] Deconinck, N. Sonderegger, P. Scaravilli, F. Vikkula, Miikka[UCL] Godfraind, Catherine[UCL] (2008) Neurology — Vol. 71, no. 1, p. 64-66 (2008)